Xenotransplantation and Risk
Regulating a Developing Biotechnology
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- Author: Sara Fovargue, Lancaster University
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Some developing biotechnologies challenge accepted legal and ethical norms because of the risks they pose. Xenotransplantation (cross-species transplantation) may prolong life but may also harm the xeno-recipient and the public due to its potential to transmit infectious diseases. These trans-boundary diseases emphasise the global nature of advances in health care and highlight the difficulties of identifying, monitoring and regulating such risks and thereby protecting individual and public health. Xenotransplantation raises questions about how uncertainty and risk are understood and accepted, and exposes tensions between private benefit and public health. Where public health is at risk, a precautionary approach informed by the harm principle supports prioritising the latter, but the issues raised by genetically engineered solid organ xenotransplants have not, as yet, been sufficiently discussed. This must occur prior to their clinical introduction because of the necessary changes to accepted norms which are needed to appropriately safeguard individual and public health.Read more
- Explores whether xenotransplantation can be accommodated within existing legal and ethical norms and looks at the legal and ethical, practical implications of allowing clinical genetically engineered solid organ xenotransplants
- Considers how risks are and can be regulated, particularly in situations of uncertainty and/or ignorance
- International and comparative aspects of the analysis facilitate the learning of relevant lessons from selected jurisdictions
Reviews & endorsements
'This book offers an up-to-date analysis and commentary of the issues pertaining to regulating xenotransplantation. Fovargue writes in a lucid, straightforward manner, without compromising on myriad complexities that surround xenotransplantation.' Nishat Hyder, Law, Innovation and Technology
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- Date Published: February 2012
- format: Adobe eBook Reader
- isbn: 9781139210461
- availability: This ISBN is for an eBook version which is distributed on our behalf by a third party.
Table of Contents
1. Introducing the issues
2. Dealing with risk
3. Regulating experimental procedures and medical research
4. Regulatory responses to developing biotechnologies
5. Challenges to legal and ethical norms: first party consent and third parties at risk
6. Surveillance and monitoring: balancing public health and individual freedom
7. Looking to the future.
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